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Clinical and molecular diagnosis of Miller-Dieker syndrome.

We report results of clinical, cytogenetic, and molecular studies in 27 patients with Miller-Dieker syndrome (MDS) from 25 families. All had severe type I lissencephaly with grossly normal cerebellum and a distinctive facial appearance consisting of prominent forehead, bitemporal hollowing, short no...

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Bibliografski detalji
Glavni autori: Dobyns, W B, Curry, C J, Hoyme, H E, Turlington, L, Ledbetter, D H
Format: Artigo
Jezik:Inglês
Izdano: 1991
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682996/
https://ncbi.nlm.nih.gov/pubmed/1671808
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